Alzheimer's disease, inflammation and non-steroidal anti-inflammatory drugs.

小胶质细胞 塞来昔布 炎症 医学 疾病 罗非昔布 神经炎症 环氧合酶 药理学 免疫学 痴呆 老年斑 阿尔茨海默病 内科学 化学 生物化学
作者
M Ferencík,M Novák,J Rovenský,I. Rybár
出处
期刊:PubMed 卷期号:102 (3): 123-32 被引量:31
链接
标识
摘要

Alzheimer's disease (AD) is a degenerative disease of the brain, which causes dementia. The disease is characterised by three main pathogenic factors: senile plaques, neurofibrillary tangles and inflammation. the participation of the local inflammatory reaction is confirmed especially by the results of studies dealing with activated microglia, reactive astrocytes, complement system, cytokines, reactive mediators of oxygen and nitrogen (free radicals), all of which participate significantly in inflammatory processes. These inflammatory markers are locally produced by brain cells, and occur in close proximity of beta-amyloid and tau protein deposits. Moreover, some epidemiologic and pilot clinical studies have proven that long-term administration of anti-inflammatory drugs have a protective effect on the onset of AD. Out of them, non-steroidal anti-inflammatory drugs (NSAIDs) are most extensively investigated medicaments. Despite some contradictory findings, the prevalent majority of these studies prove that long-term application of anti-inflammatory treatment can delay the onset, or at least slow down the progression of AD, namely in people between 65 and 75 years of age. The most appropriate prophylactic effect seems to be achieved by specific inhibitors of cyclooxygenase-2 (COX-2), namely celecoxib and rofecoxib. These preparations protect the gastrointestinal tract better than classical NSAIDs which inhibit both isoenzymes--COX-1 and COX-2. COX-2 is expressed in higher concentrations in the degenerating cells of the brain and this excessive expression can be decreased by selective inhibitors. The latter decrease also the excessive activation of some transcription factors (PPARgama and the nuclear factor kapa-B), which are responsible for the initiation of transcription of a number of pro-inflammatory genes. The selective inhibitors COX-2 can thereby have an anti-inflammatory effect operating on several levels. (Tab. 1, Fig. 1, Ref. 75.)

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
1秒前
学术蝗虫完成签到 ,获得积分10
1秒前
睡不着发布了新的文献求助10
2秒前
独特的忆彤完成签到 ,获得积分10
2秒前
3秒前
3秒前
高兴断秋完成签到,获得积分10
3秒前
请输入昵称完成签到 ,获得积分10
4秒前
godblessyou应助大笨蛋采纳,获得10
4秒前
5秒前
6秒前
PINKPIG发布了新的文献求助10
6秒前
6秒前
shellytingxie发布了新的文献求助10
7秒前
piaopiao完成签到,获得积分10
8秒前
9秒前
小青完成签到,获得积分10
9秒前
刘尚琴发布了新的文献求助10
10秒前
星星醒醒发布了新的文献求助10
10秒前
qphys完成签到,获得积分0
10秒前
10秒前
11秒前
Freedom完成签到 ,获得积分10
12秒前
科研通AI6.2应助咖喱采纳,获得10
12秒前
12秒前
卫乐天完成签到,获得积分10
13秒前
科研通AI6.1应助PINKPIG采纳,获得10
13秒前
14秒前
op06d发布了新的文献求助10
15秒前
16秒前
Lee_Ding_95发布了新的文献求助10
16秒前
CipherSage应助nanxin采纳,获得10
18秒前
林夕完成签到,获得积分10
19秒前
lzcnextdoor发布了新的文献求助10
19秒前
Yuki完成签到 ,获得积分10
20秒前
打打应助shellytingxie采纳,获得10
21秒前
lzcnextdoor完成签到,获得积分10
23秒前
暴躁的嘉懿完成签到,获得积分10
25秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
卤化钙钛矿人工突触的研究 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6515939
求助须知:如何正确求助?哪些是违规求助? 8308943
关于积分的说明 17759304
捐赠科研通 5618111
什么是DOI,文献DOI怎么找? 2925273
邀请新用户注册赠送积分活动 1902286
关于科研通互助平台的介绍 1763498